多路复用
核酸检测
病毒学
核酸
多重聚合酶链反应
生物
核酸扩增试验
清脆的
RNA提取
核糖核酸
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
聚合酶链反应
医学
疾病
生物信息学
基因
遗传学
传染病(医学专业)
病理
沙眼衣原体
作者
Jia Li,Nan Li,Li Zhang,Ying Lu,Minjie Shen,Yuanyue Zhang,Feng Li,Juhui Jing,Jing Cheng,Youchun Xu
标识
DOI:10.1002/smtd.202400030
摘要
Abstract High‐quality, low‐cost, and rapid detection is essential for the society to reopen the economy during the critical period of transition from Coronavirus Disease 2019 (COVID‐19) pandemic response to pandemic control. In addition to performing sustainable and target‐driven tracking of SARS‐CoV‐2, conducting comprehensive surveillance of variants and multiple respiratory pathogens is also critical due to the frequency of reinfections, mutation immune escape, and the growing prevalence of the cocirculation of multiple viruses. By utilizing a 0.05 cents wax interface, a Stable Interface assisted Multiplex Pathogenesis Locating Estimation in Onepot (SIMPLEone) using nested RPA and CRISPR/Cas12a enzymatic reporting system is successfully developed. This smartphone‐based SIMPLEone system achieves highly sensitive one‐pot detection of SARS‐CoV‐2 and its variants, or multiple respiratory viruses, in 40 min. A total of 89 clinical samples, 14 environmental samples, and 20 cat swab samples are analyzed by SIMPLEone, demonstrating its excellent sensitivity (3–6 copies/reaction for non‐extraction detection of swab and 100–150 copies/mL for RNA extraction‐based assay), accuracy (>97.7%), and specificity (100%). Furthermore, a high percentage (44.2%) of co‐infection cases are detected in SARS‐CoV‐2‐infected patients using SIMPLEone's multiplex detection capability.
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